Composition for preventing or treating glioblastoma comprising Platycodon grandiflorum A. De Candolle, Scutellaria baicalensis, Phellodendron amurense Ruprecht or Rubus coreanus
a technology of glioblastoma and composition, which is applied in the direction of medical preparations, plant ingredients, plant/algae/fungi/lichens ingredients, etc., to achieve the effects of inhibiting the growth of gbm, preventing, improving, or treating gbm
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example 7
Immunofluorescence Analysis
[0128]Cells treated with the materials were permeabilized with 0.01% Triton X-100 in PBS. After blocking the resulting cells in 2% bovine serum albumin (BSA) in PBS, they were incubated at 4° C. with a primary antibody against SQSTM1 / p62 (Santa Cruz) overnight. The stained cells were incubated with an Alexa594-conjugated secondary antibody (Invitrogen, Calif., USA). The images were examined under a Zeiss laser confocal microscope.
example 8
Lysotracker Assay
[0129]To stain acidic compartments, 50 nM LysoTrackerRedDND-99 (Thermo Fisher Scientific) was added to a medium at 37° C. with 5% CO2 for 30 minutes prior to fixation. The nuclei were labeled with 4,6-diamidino-2-phenylindole (DAPI, Sigma). The slides were finally mounted using a Faramount mounting medium (Dako, Glostrup, Denmark). The images were examined under a Zeiss laser confocal microscope.
example 9
DO Red-BSA Trafficking Assay
[0130]Cells were placed on coverslips prior to treatment with the materials and continuously loaded with DQ Red-BSA (Invitrogen) at a working concentration of 10 μg / mL in a culture medium at 37° C. for 30 minutes. The cells were fixed in 4% PFA and then subjected to DAPI staining. The images were examined under a Zeiss laser confocal microscope. The number of DQ Red-BSA spots was quantified using ImageJ software.
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